HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3059Erstellt: 25. Oktober 2026
Hydrochloric Acid → 2-Methyl-2,3-dihydro-1-benzofuran-5-carboxylic acid
https://huagongshe.com/reaction/3059
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Bromine | HCID 24408 | — |
| Edukt | 1-(2-Methyl-2,3-dihydro-1-benzofuran-5-yl)ethan-1-one | HCID 42799 | — |
| Edukt | Hypobromous acid | HCID 83547 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 2-Methyl-2,3-dihydro-1-benzofuran-5-carboxylic acid | HCID 647255 | 57,4% |
Reaktionsschritte
On an ice-common salt bath, 6.25 ml of bromine was added dropwise to a solution of 15.1 g of sodium hydroxide in 100 ml of water under stirring and cooling. To a solution of 6.50 g of 5-acetyl-2-methyl coumaran (Ml) in 100 ml of dioxane, the above mixture (i.e., hypobromous acid solution) was added dropwise at 3°-8° C. under cooling on an ice bath. The ice bath was removed after the addition. The resultant mixture was stirred for 3.5 hours at room temperature. After the reaction, the reaction mixture was poured into 500 ml of ice water, followed by addition of 30 ml of hydrochloric acid to precipitate a crystal. The crystal was recovered by filtration and washed with water. The resultant crystal was dried under reduced pressure, followed by washing with hexane and isopropyl ether successively to obtain 3.77 g of 5-carboxy-2-methylcoumaran (M2) (Yield: 57.4%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05733476 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-2219c1d1d75847559c21756e148ff10b |
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| Quellennotiz | uspto-grants-1998_03 |
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